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T68124Pafenolol；帕非洛尔Pafenolol
Pafenolol is a P-glycoprotein modulator with a Ki value of 5.5 ?M. pafenolol is an orally available and selective beta-adrenergic receptor antagonist.
价 格：￥电议型 号：T68124产 地：中国大陆
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T6766Atipamezole阿替美唑Antisedan|||阿替美唑|||MPV 1248
Atipamezole (Antisedan) is a synthetic α2 adrenergic receptor antagonist. It has also been researched in humans as a potential anti-Parkinsonian drug.
价 格：￥电议型 号：T6766产 地：中国大陆
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T6765Atipamezole hydrochloride；阿替美唑盐酸盐MPV-1248 hydrochloride|||Antisedan；阿替美唑盐酸盐|||MPV-1248 hydrochloride
Atipamezole is a synthetic α2 adrenergic receptor antagonist. It has also been researched in humans as a potential anti-Parkinsonian drug. Atipamezole hydrochloride (MPV-1248 hydrochloride) is hydrochloride form of atipamezole.
价 格：￥电议型 号：T6765产 地：中国大陆
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T6755AM1241；化合物AM1241AM1241
AM-1241 is a selective cannabinoid CB2 receptor agonist with Ki of 3.4 nM, exhibits 82-fold selectivity over CB1 receptor.
价 格：￥电议型 号：T6755产 地：中国大陆
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T671242-Dodecanamidoacetic acid；化合物 2-Dodecanamidoacetic acid2-Dodecanamidoacetic acid
2-Dodecanamidoacetic acid is a useful organic compound for research related to life sciences and the catalog number is T67124.
价 格：￥电议型 号：T67124产 地：中国大陆
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T6658SB-408124化合物SB408124N-(6,8-二氟-2-甲基-4-喹啉)- N-[4-(二甲氨基)苯基]尿素
SB408124 is a non-peptide antagonist for OX1 receptor with Ki of 57 nM and 27 nM in both whole cell and membrane, respectively, exhibits 50-fold selectivity over OX2 receptor.
价 格：￥电议型 号：T6658产 地：中国大陆
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T661242′-Fluoroacetophenone；化合物 2′-Fluoroacetophenone2′-Fluoroacetophenone
2′-Fluoroacetophenone is a useful organic compound for research related to life sciences. The catalog number is T66124 and the CAS number is 445-27-2.
价 格：￥电议型 号：T66124产 地：中国大陆
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T65124Dipentamethylenethiuram Tetrasulfide；化合物 Dipentamethylenethiuram TetrasulfideDipentamethylenethiuram
Dipentamethylenethiuram Tetrasulfide is a useful organic compound for research related to life sciences. The catalog number is T65124 and the CAS number is 120-54-7.
价 格：￥电议型 号：T65124产 地：中国大陆
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T6509Galeterone；化合物GaleteroneVN-124-1|||TOK-001|||VN/124-1|||VN 124；VN-124-1|||TOK-001|||VN/124-1|||VN 12
Galeterone (VN 124) is an orally bioavailable small-molecule androgen receptor modulator and CYP17 lyase inhibitor with potential antiandrogen activity. Galeterone exhibits three distinct mechanisms of action: 1) as an androgen receptor antagonist, 2) as a CYP17 lyase inhibitor and 3) by decreasing overall androgen receptor levels in prostate cancer tumors, all of which may result in a decrease in androgen-dependent growth signaling. Localized to the endoplasmic reticulum (ER), the cytochrome P4
价 格：￥电议型 号：T6509产 地：中国大陆
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T65062Carbostyril 124；化合物 Carbostyril 124Carbostyril 124
Carbostyril 124 is a useful organic compound for research related to life sciences. The catalog number is T65062 and the CAS number is 19840-99-4.
价 格：￥电议型 号：T65062产 地：中国大陆
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T64573Stat3 (124H6) Mouse mAb #9139M；化合物 Stat3 (124H6) Mouse mAb #9139MStat3 (124H6) Mouse mAb #9139M
Stat3 (124H6) Mouse mAb #9139M is a useful organic compound for research related to life sciences and the catalog number is T64573.
价 格：￥电议型 号：T64573产 地：中国大陆
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T64293SLN124；化合物 SLN124SLN124
SLN124 is a GalNac-siRNA that targets transmembrane serine protease 6 (Tmprss6) and consists of a trimeric GalNAc ligand bound to TMPRSS6-siRNA. SLN124 has the potential to be used as an siRNA agent to restore ferroregulatory expression and normalize iron homeostasis in β-depletion.
价 格：￥电议型 号：T64293产 地：中国大陆
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T64124Sunvozertinib；舒沃替尼DZD9008|||DZD 9008|||DZD-9008；DZD9008|||DZD 9008|||DZD-9008
Sunvozertinib (DZD9008) is a potent ErbBs and BTK inhibitor and has inhibitory effects on EGFR, Her2 and mutant epidermal growth factor. Sunvozertinib showed inhibition of EGFR exon 20 NPH insertion, EGFR exon 20 ASV insertion, EGFR L858R and T790M mutation, and Her2 exon 20 YVMA and EGFR WT A431. IC50 were 20.4, 20.4, 1.1, 7.5 and 80.4 nM, respectively.
价 格：￥电议型 号：T64124产 地：中国大陆
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T6350CHIR-124；化合物CHIR124CHIR124|||CHIR 124；CHIR124|||CHIR 124
CHIR-124 is an effective Chk1 inhibitor (IC50: 0.3 nM). It has 2, 000-fold selectivity against Chk2, 500- to 5, 000-fold less activity against Cdc2 and CDK2/4.
价 格：￥电议型 号：T6350产 地：中国大陆
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T63206SR12418；化合物 SR12418SR12418
SR12418 is a specific REV-ERB synthetic ligand that acts on REV-ERBα (IC50: 68 nM) and REV-ERBβ (IC50: 119 nM) and can be used to study experimental autoimmune encephalomyelitis (EAE) and colitis.
价 格：￥电议型 号：T63206产 地：中国大陆
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T63124RORγt modulator 4；化合物 RORγt modulator 4RORγt modulator 4
RORγt modulator 4 is a RORγt modulator that regulates IL-17A production activity in cells derived from mouse spleen.
价 格：￥电议型 号：T63124产 地：中国大陆
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T6283Wortmannin；渥曼青霉素SL-2052|||KY-12420；SL-2052|||渥曼青霉素|||KY-12420
Wortmannin (SL-2052) is a PI3K inhibitor (IC50=3 nM) that is covalent and irreversible. Wortmannin is also an inhibitor of PlK1 and PlK3 (IC50=5.8/48 nM) that blocks autophagy.
价 格：￥电议型 号：T6283产 地：中国大陆
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T62124Anticancer agent 80；化合物 Anticancer agent 80Anticancer agent 80
Anticancer agent 80 (Compound 3c) is an anticancer agent that exhibits a significant dark toxic effect on T47-D (IC50: 10.14 μM).
价 格：￥电议型 号：T62124产 地：中国大陆
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T61249α-Glucosidase-IN-2；化合物 α-Glucosidase-IN-2α-Glucosidase-IN-2
α-Glucosidase-IN-2 (compound 5d) is a potent inhibitor of α-Glucosidase, exhibiting an inhibitory concentration (IC50) of 9.48 μM, and functions as an antidiabetic agent [1].
价 格：￥电议型 号：T61249产 地：中国大陆
